Frontiers Case report: A preterm infant with rubinstein-taybi

The Rubinstein-Taybi syndrome: a report of two cases.

Frontiers Emergent Prophylactic, Reparative and Restorative Brain Interventions for Infants Born Preterm With Cerebral Palsy

Frontiers in Pediatrics

novel frameshift mutation - List of Frontiers' open access articles

novel frameshift mutation - List of Frontiers' open access articles

A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with Atypical Rubinstein–Taybi Syndrome Phenotypes

Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant

JPM, Free Full-Text

Inhibition of Histone Deacetylases 1, 2, and 3 Enhances Clearance of Cholesterol Accumulation in Niemann-Pick C1 Fibroblasts

PDF] Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the SLX4, DNASE1, TRAP1, and CREBBP Genes Presenting as a Relatively Mild Rubinstein–Taybi Syndrome Phenotype: A Case Report of a Saudi Boy

Frontiers in Pediatrics Genetics of Common and Rare Diseases

Frontiers in Pediatrics

Frontiers in Pediatrics Genetics of Common and Rare Diseases

Frontiers The effects of early combined training on the physical development of preterm infants with different gestational ages

Frontiers Impact of Comorbid Prematurity and Congenital Anomalies: A Review